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作 者:Weili Wang Hao Ma Qiuting Huang Siheng Luo Bin Ren Zhongqun Tian Guokun Liu
机构地区:[1]State Key Laboratory of Marine Environmental Science,Fujian Provincial Key Laboratory for Coastal Ecology and Environmental Studies,Center for Marine Environmental Chemistry and Toxicology,College of the Environment and Ecology,Xiamen University,Xiamen,Fujian,China [2]State Key Laboratory for Physical Chemistry of Solid Surfaces,College of Chemistry and Chemical Engineering,Xiamen University,Xiamen,Fujian,China
出 处:《Aggregate》2024年第5期394-401,共8页聚集体(英文)
基 金:National Natural Science Foundation,Grant/Award Numbers:22272139,22227802,22021001,22104125;China Postdoctoral Science Foundation,Grant/Award Number:2021M691870。
摘 要:Existential state of solutes substantially affects the efficiency and direction of vari-ous chemical and biological processes,about which current consensus is still limited at macro and micro levels.At the trace level,solutes assume a pivotal role across a spectrum of criticalfields.However,their existential states,especially at inter-faces,remain largely elusive.Herein,an exceptional evolution of solute molecules is unveiled from micro to trace,solution to interface,with the aid of surface-enhanced Raman spectroscopy,extinction,DLS and theoretical simulations.Given predom-inant existence of monomers within the solution,these aggregates dominate the interfacial behavior of solute molecules.Moreover,a universal,aggregate-controlled mechanism is demonstrated that aggregates triggered by cosolvent,which can dra-matically promote efficiency of catalytic reactions.The results provide novel insights into the interaction mechanisms between reactants and catalysts,potentially offering fresh perspectives for the manipulation of multiphase catalysis and related biological processes.
关 键 词:AGGREGATE molecular dynamics surface-enhanced Raman spectroscopy
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